- Imaging of Thoracic Wall Abnormalities
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Semionov A, Kosiuk J, Ajlan A, Discepola
- KMID: 2459163
- Korean J Radiol.
- 2019 Oct;20(10):1441-1453.
- doi: 10.3348/kjr.2019.0181
Identification of certain abnormalities of the chest wall can be extremely helpful in correctly diagnosing a number of syndromic conditions and systemic diseases. Additionally, chest wall abnormalities may sometimes constitute... -
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- Microcytosis in children and adolescents with the sickle cell trait in Basra, Iraq
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Jaber RZ, Hassan MK, Al-Salait
- KMID: 2451054
- Blood Res.
- 2019 Mar;54(1):38-44.
- doi: 10.5045/br.2019.54.1.38
BACKGROUND: Microcytic anemia, the most common form of anemia in children and adolescents, is a heterogeneous group of diseases that is acquired or inherited. We assessed the frequency and causes... -
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- Recent progress in laboratory diagnosis of thalassemia and hemoglobinopathy: a study by the Korean Red Blood Cell Disorder Working Party of the Korean Society of Hematology
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Lee YK, Kim HJ, Lee K, Park SH, Song SH, Seong MW, Kim M, Han JY
- KMID: 2451051
- Blood Res.
- 2019 Mar;54(1):17-22.
- doi: 10.5045/br.2019.54.1.17
Genetic hemoglobin disorders are caused by mutations and/or deletions in the α-globin or β-globin genes. Thalassemia is caused by quantitative defects and hemoglobinopathies by structural defect of hemoglobin. The incidence... -
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- Increased Prevalence of Thalassemia in Young People in Korea: Impact of Increasing Immigration
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Lee HJ, Shin KH, Kim HH, Yang EJ, Park KH, Kim MJ, Kwon JR, Choi YS, Kim JN, Shin MG, Cho YG, Kim SJ, Kim KH, Jeong S, Kong SG, Jung YJ, Lee N, Kim MJ, Seong MW
- KMID: 2425968
- Ann Lab Med.
- 2019 Mar;39(2):133-140.
- doi: 10.3343/alm.2019.39.2.133
BACKGROUND: Thalassemia is highly prevalent in Southeast Asia but is rare in Korea; however, Southeast Asian immigrant population is recently rising in Korea. We investigated the prevalence of thalassemia in... -
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- Relationship between liver iron concentration determined by R2-MRI, serum ferritin, and liver enzymes in patients with thalassemia intermedia
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Al-Momen H, Jasim SK, Hassan QA, Ali HH
- KMID: 2429306
- Blood Res.
- 2018 Dec;53(4):314-319.
- doi: 10.5045/br.2018.53.4.314
BACKGROUND: Iron overload is a risk factor affecting all patients with thalassemia intermedia (TI). We aimed to determine whether there is a relationship of serum ferritin (SF) and alanine aminotransferase... -
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- Allogeneic hematopoietic stem cell transplantation in congenital hemoglobinopathies with myeloablative conditioning and rabbit anti-thymocyte globulin
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Park BK, Kim HS, Kim S, Lee JW, Park YS, Jang PS, Chung NG, Jeong DC, Cho B
- KMID: 2451033
- Blood Res.
- 2018 Jun;53(2):145-151.
- doi: 10.5045/br.2018.53.2.145
BACKGROUND: Allogeneic hematopoietic stem cell transplantation (HSCT) is a curative therapy for β-thalassemia major (TM) and sickle cell disease (SCD) in children. Graft-versus-host disease (GVHD) and treatment-related mortality (TRM) remain... -
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- The Effect of ABO Blood Groups, Hemoglobinopathy, and Heme Oxygenase-1 Polymorphisms on Malaria Susceptibility and Severity
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Kuesap J, Na-Bangchang K
- KMID: 2412735
- Korean J Parasitol.
- 2018 Apr;56(2):167-173.
- doi: 10.3347/kjp.2018.56.2.167
Malaria is one of the most important public health problems in tropical areas on the globe. Several factors are associated with susceptibility to malaria and disease severity, including innate immunity... -
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- Depression, Anxiety, and Perceived Social Support among Adults with Beta-Thalassemia Major: Cross-Sectional Study
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Maheri A, Sadeghi R, Shojaeizadeh D, Tol A, Yaseri M, Rohban A
- KMID: 2411631
- Korean J Fam Med.
- 2018 Mar;39(2):101-107.
- doi: 10.4082/kjfm.2018.39.2.101
BACKGROUND: Considering the high prevalence of depression and anxiety among thalassemia patients and the role of social support in preventing mental disorders, this study aimed to determine prevalence of depression,... -
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- Does the c.-273T>C variant in the upstream region of the HBB gene cause a thalassemia phenotype?
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Dastsooz H, Alipour M, Mohammadi , Dehghanian F, Kamgarpour F, Fardaei M
- KMID: 2405076
- Blood Res.
- 2017 Dec;52(4):332-334.
- doi: 10.5045/br.2017.52.4.332
No abstract available. -
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- A Case of Pregnant Woman with beta-Thalassemia in Korean
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Ryu A
- KMID: 2404862
- Soonchunhyang Med Sci.
- 2017 Dec;23(2):143-145.
- doi: 10.0000/sms.2017.23.2.143
Thalassemia is hereditary disease characterized by impaired production of the normal globin peptide. Beta-thalassemia, a common disorder in Central Africa, the Middle East, and Southeast Asia, has been rarely reported... -
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- A Survey of the Opinions of Transfusion Specialists on Transfusion Policy of Thalassemia Patients in Korea
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Lee HJ, Shin KH, Kim HH, Kim MJ, Kim JN
- KMID: 2401746
- Korean J Blood Transfus.
- 2017 Dec;28(3):282-289.
- doi: 10.17945/kjbt.2017.28.3.282
BACKGROUND: Thalassemia patients are treated with chronic blood transfusion to relief symptoms. The prevalence of thalassemia in Korea has been increasing recently in response to an increase in the number... -
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- 2 Cases of Beta-thalassemia Minor in Korea
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Kim EJ, Jeung SW, Yoon HS
- KMID: 2396015
- Clin Pediatr Hematol Oncol.
- 2017 Oct;24(2):136-139.
- doi: 10.15264/cpho.2017.24.2.136
In Korea, recent epidemiologic studies show that the incidence of β-thalassemia is increasing as the influx of South-East Asian population increases and molecular technologies develop. However, many patients are still... -
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- An Analysis of Blood Utilization for Stem Cell Transplant Patients in a Tertiary Care Hospital
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Ali N
- KMID: 2384608
- Int J Stem Cells.
- 2017 May;10(1):114-118.
- doi: 10.15283/ijsc16045
BACKGROUND AND OBJECTIVE: Haematopoietic stem cell transplant is a potentially curative treatment option in various benign and malignant haematological diseases. Patients undergoing stem cell transplant procedure require blood transfusion on... -
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- Human parvovirus B19 in patients with beta thalassemia major from Tehran, Iran
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Arabzadeh , Alizadeh F, Tavakoli A, Mollaei H, Bokharaei-Salim F, Karimi G, Farahmand , Mortazavi , Monavari S
- KMID: 2375204
- Blood Res.
- 2017 Mar;52(1):50-54.
- doi: 10.5045/br.2017.52.1.50
BACKGROUND: Due to the tropism of human parvovirus B19 to erythroid progenitor cells, infection in patients with an underlying hemolytic disorder such as beta-thalassemia major leads to suppression of erythrocyte... -
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- Poor quality of life as a predictor of survival among thalassemia patients in Iran
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Rezaeian S
- KMID: 2406617
- Epidemiol Health.
- 2017;39:e2017013.
- doi: 10.4178/epih.e2017013
No abstract available. -
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- Iron-deficiency anemia in children: from diagnosis to treatment
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Lee JH
- KMID: 2391983
- J Korean Med Assoc.
- 2016 Sep;59(9):678-682.
- doi: 10.5124/jkma.2016.59.9.678
Iron-deficiency anemia (IDA) is the most frequent hematologic and nutritional disorder in children. The risk factors associated with IDA in children are rapid growth with inadequate dietary iron, low birth... -
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- Delta beta thalassemia: a rare hemoglobin variant
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Mansoori H, Asad S, Rashid A, Karim F
- KMID: 2353507
- Blood Res.
- 2016 Sep;51(3):213-214.
- doi: 10.5045/br.2016.51.3.213
No abstract available. -
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- Effectiveness of premarital screening program for thalassemia and sickle cell disorders in Ras Al Khaimah, United Arab Emirates
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Salama RA, Saleh AK
- KMID: 2327699
- J Genet Med.
- 2016 Jun;13(1):26-30.
- doi: 10.5734/JGM.2016.13.1.26
PURPOSE: Genetic disorders can be prevented by basic public health measures and activities that focus primarily on education and approaches in Primary Health Care. Premarital screening is one such approach... -
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- Treatment and Management of Late Complications in Hereditary Hemolytic Anemia
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Chueh HW
- KMID: 2168902
- Clin Pediatr Hematol Oncol.
- 2016 Apr;23(1):1-7.
- doi: 10.15264/cpho.2016.23.1.1
Hereditary hemolytic anemia is a very heterogeneous disorder in which abnormalities of red blood cell structural protein, globin protein, or enzyme defect lead to shortened life span. There has been... -
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- Associations between a health-promoting lifestyle and quality of life among adults with beta-thalassemia major
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Maheri A, Sadeghi R, Shojaeizadeh D, Tol A, Yaseri M, Ebrahimi M
- KMID: 2380738
- Epidemiol Health.
- 2016;38:e2016050.
- doi: 10.4178/epih.e2016050
OBJECTIVES: A health-promoting lifestyle (HPL) is a factor that affects the quality of life (QoL) in patients with beta-thalassemia (β-thalassemia). Due to the lack of studies of this issue, this... -
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